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Sandhoff disease, infantile form | RareConnect | RareConnect.io

/Sandhoff disease

/Sandhoff disease, infantile form

Sandhoff disease, infantile form

Rare Disease

MONDO:0017721

Also Known As

Hexosaminidases A and B deficiency, infantile forminfantile GM2 gangliosidosis 0 variant

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External Resources

Orphanet

Orphanet:309155 ↗

GARD

Related Diseases

Sandhoff disease, juvenile form

MONDO:0017722

Sandhoff disease, adult form

MONDO:0017723

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